rs587782329, TP53

N. diseases: 7
Source: BEFREE ×
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
cervical cancer
CUI: C4048328
Disease: cervical cancer
257 0.677 0.280 17 7674217 missense variant C/A;G;T snv 0.020 1.000 2 2000 2004
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
266 0.677 0.280 17 7674217 missense variant C/A;G;T snv 0.020 1.000 2 2000 2004
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.677 0.280 17 7674217 missense variant C/A;G;T snv 0.020 1.000 2 2000 2004
Carcinoma in situ of uterine cervix
CUI: C0851140
Disease: Carcinoma in situ of uterine cervix
18 0.677 0.280 17 7674217 missense variant C/A;G;T snv 0.010 1.000 1 2000 2000
Cervix Diseases
CUI: C0007867
Disease: Cervix Diseases
3 0.677 0.280 17 7674217 missense variant C/A;G;T snv 0.010 1.000 1 2017 2017
High-Grade Squamous Intraepithelial Lesions
CUI: C0333875
Disease: High-Grade Squamous Intraepithelial Lesions
8 0.677 0.280 17 7674217 missense variant C/A;G;T snv 0.010 1.000 1 2017 2017
Lung Neoplasms
CUI: C0024121
Disease: Lung Neoplasms
39 0.677 0.280 17 7674217 missense variant C/A;G;T snv 0.010 1.000 1 1997 1997